Author: Kenneth Michael BeckPublisher:
ISBN:
Category :
Languages : en
Pages : 440
Book Description
Vibrational Relaxation of Excited and Highly Excited Polyatomic Molecules
Author: Kenneth Michael BeckPublisher:
ISBN:
Category :
Languages : en
Pages : 440
Book Description
The Vibrational Relaxation of Highly Excited Polyatomic Molecules
Author: John VlahoyannisLaser Spectroscopy of Highly Vibrationally Excited Molecules
Author: Vladilen Stepanovich LetokhovPublisher: CRC Press
ISBN: 1000445127
Category : Science
Languages : en
Pages : 397
Book Description
Laser spectroscopy has been perfected over the last fifteen years to become a precise tool for the investigation of highly vibrationally excited molecules. Intense infrared laser radiation permits both the multiple-photon resonant excitation and the dissociation of polyatomic molecules. In this book, the latest results of some of the foremost Soviet researchers are published for the first time in the West. Laser Spectroscopy of Highly Vibrationally Excited Molecules contains a comprehensive study of both the experimental and theoretical aspects of the basic photophysical interactions that occur in these processes. The book first focuses on the nonlinear interaction between the resonant vibrational mode and the intense infrared field and then examines the nonlinear interaction between the vibrational modes themselves due to anharmonicity. These interrelated processes determine all the characteristics of polyatomic molecules in an infrared field. The book also discusses related phenomena such as spectra broadening, optical resonance, photon echoes, and dynamical chaos. It includes examples of multiple-photon resonant excitation such as the excitation of OsO4 by CO^O2 laser radiation, which is detected by the visible luminescence that results. This book will be of great interest to researchers and postgraduate students in infrared laser spectroscopy and the laser chemistry of molecules and applications of isotope separation.
Vibrational State Mixing and Vibrational Relaxation of Electronically Excited Polyatomic Molecules
Author: Desmond John MullerPublisher:
ISBN:
Category : Vibration
Languages : en
Pages :
Book Description
Highly Excited Molecules
Author: Amy S. MullinPublisher:
ISBN:
Category : Science
Languages : en
Pages : 352
Book Description
Integrating both theoretical and experimental approaches, this unique book examines transition states and chemical reactivity, and will be a useful tool for anyone studying the chemical dynamics, nature, and behavior of molecules in an excited state. The subject has important applications in atmospheric chemistry, plasmas, high-temperature materials processing, combustion, photosynthesis, detonation, and explosives.
State-Resolved Collisional Energy Transfer in Highly Vibrationally Excited Polyatomic Molecules
Author: Publisher:
ISBN:
Category :
Languages : en
Pages : 17
Book Description
The transfer of energy in isolated or colliding molecules is a fundamental process with practical consequences for complex phenomena occurring in atmospheric chemistry, combustion, molecular lasers, plasmas, and a host of other environments containing energetic species. We have developed a technique that combines vibrational overtone excitation, to prepare highly vibrationally excited initial states, and time-resolved spectroscopic detection, to probe the evolution of the prepared state, for studying energy transfer in vibrationally energized molecules. We have used this approach to determine directly, for the first time, the frequencies of the three ungerade vibrations in the first electronically excited state of acetylene. Using this information we have characterized highly vibrationally excited states of acetylene and directly the frequencies and rotational constants of the perturbing vibrational states at these energies. Combining these spectroscopic insights on the vibrationally and electronically excited states of acetylene has allowed us to determine the energy transfer rates and pathways in the collisional relaxation of a polyatomic molecule containing 10,000 cm-1 of vibrational energy, Rotational energy transfer is very rapid, occurring on about every other collision, but is essentially unaffected by the identity of the vibrational state in which the rotational relaxation occurs.
Collisional Energy Transfer in Highly Vibrationally Excited Polyatomic Molecules
Author: F. F. CrimPublisher:
ISBN:
Category :
Languages : en
Pages : 22
Book Description
The three objectives of this work are to determine the nature of highly vibrationally excited polyatomic molecule, to determine the rate constants and pathways for the collisional relaxation of these molecules, and to probe the electronic spectroscopy of these molecules. We have created and implemented approaches for accomplishing these objectives and have demonstrated their feasibility by studying the collisional energy transfer in highly vibrational excited acetylene. We have found that the collisional self relaxation rates of single angular momentum states with 10,000/cm of vibrational energy are a substantial fraction of the gas kinetic collision rates. The rate constant is about a factor of two smaller for relaxation by atomic partners. Molecular energy transfer, Vibrational energy transfer. (MJM).
Laser Spectroscopy of Highly Vibrationally Excited Molecules
Author: Vladilen Stepanovich LetokhovPublisher: CRC Press
ISBN: 1000447855
Category : Science
Languages : en
Pages : 358
Book Description
Laser spectroscopy has been perfected over the last fifteen years to become a precise tool for the investigation of highly vibrationally excited molecules. Intense infrared laser radiation permits both the multiple-photon resonant excitation and the dissociation of polyatomic molecules. In this book, the latest results of some of the foremost Soviet researchers are published for the first time in the West. Laser Spectroscopy of Highly Vibrationally Excited Molecules contains a comprehensive study of both the experimental and theoretical aspects of the basic photophysical interactions that occur in these processes. The book first focuses on the nonlinear interaction between the resonant vibrational mode and the intense infrared field and then examines the nonlinear interaction between the vibrational modes themselves due to anharmonicity. These interrelated processes determine all the characteristics of polyatomic molecules in an infrared field. The book also discusses related phenomena such as spectra broadening, optical resonance, photon echoes, and dynamical chaos. It includes examples of multiple-photon resonant excitation such as the excitation of OsO4 by CO^O2 laser radiation, which is detected by the visible luminescence that results. This book will be of great interest to researchers and postgraduate students in infrared laser spectroscopy and the laser chemistry of molecules and applications of isotope separation.
Topics in Fluorescence Spectroscopy
Author: Joseph R. LakowiczPublisher: Springer Science & Business Media
ISBN: 0306470705
Category : Science
Languages : en
Pages : 555
Book Description
Fluorescence spectroscopy continues its advance to more sophisticated methods and applications. As one looks over the previous decades, its appears that the first practical instruments for time-resolved measurements appeared in the 1970’s. The instrumentation and analysis methods for time-resolved fluorescence advanced rapidly throughout the 1980’s. Since 1990 we have witnessed a rapid migration of the principles of time-resolved fluorescence to cell biology and clinical appli- tions. Most recently, we have seen the introduction of multi-photon excitation, pump-probe and stimulated emission methods for studies of biological mac- molecules and for cellular imaging. These advanced topics are the subject of the present volume. Two-photon excitation was first predicted by Maria Goppert-Mayer in 1931, but was not experimentally observed until 1961. Observation of two-photon excitation required the introduction of lasers which provided adequate photon density for multi-photon absorption. Since the early observations of two-photon excitation in the 1960s, multi-photon spectroscopy has been limited to somewhat exotic applications of chemical physics, where it is used to study the electronic symmetry of small molecules. Placing one’s self back in 1980, it would be hard to imagine the use of multi-photon excitation in biophysics or cellular imaging.
Strategies for Planar Laser-induced Fluorescence Thermometry in Shock Tube Flows
Author: Ji Hyung YooPublisher: Stanford University
ISBN:
Category :
Languages : en
Pages : 151
Book Description
This thesis was motivated by the need to better understand the temperature distribution in shock tube flows, especially in the near-wall flow regions. Two main ideas in planar laser-induced fluorescence (PLIF) diagnostics are explored in this thesis. The first topic is the development of a single-shot PLIF diagnostic technique for quantitative temperature distribution measurement in shock tube flow fields. PLIF is a non-intrusive, laser-based diagnostic technique capable of instantaneously imaging key flow features, such as temperature, pressure, density, and species concentration, by measuring fluorescence signal intensity from laser-excited tracer species. This study performed a comprehensive comparison of florescence tracers and excitation wavelengths to determine the optimal combination for PLIF imaging in shock tube flow applications. Excitation of toluene at 248nm wavelength was determined to be the optimal strategy due to the resulting high temperature sensitivity and fluorescence signal level, compared to other ketone and aromatic tracers at other excitation wavelengths. Sub-atmospheric toluene fluorescence yield data was measured to augment the existing photophysical data necessary for this diagnostic technique. In addition, a new imaging test section was built to allow PLIF imaging in all regions of the shock tube test section, including immediately adjacent to the side and end walls. The signal-to-noise (SNR) and spatial resolution of the PLIF images were optimized using statistical analysis. Temperature field measurements were made with the PLIF diagnostic technique across normal incident and reflected shocks in the shock tube core flow. The resulting images show uniform spatial distribution, and good agreement with conditions calculated from the normal shock jump equations. Temperature measurement uncertainty is about 3.6% at 800K. The diagnostic was also applied to image flow over a wedge. The resulting images capture all the flow features predicted by numerical simulations. The second topic is the development of a quantitative near-wall diagnostic using tracer-based PLIF imaging. Side wall thermal boundary layers and end wall thermal layers are imaged to study the temperature distribution present under constant pressure conditions. The diagnostic technique validated in the shock tube core flow region was further optimized to improve near-wall image quality. The optimization process considered various wall materials, laser sheet orientations, camera collection angles, and optical components to find the configuration that provides the best images. The resulting images have increased resolution (15[Mu]m) and are able to resolve very thin non-uniform near-wall temperature layers (down to 60[Mu]m from the surface). The temperature field and thickness measurements of near-wall shock tube flows under various shock conditions and test gases showed good agreement with boundary layer theory. To conclude this thesis, new applications and future improvements to the developed PLIF diagnostic technique are discussed. These suggested refinements can provide an even more robust and versatile PLIF imaging technique capable of measuring a wider range of flow conditions near walls.